檢索結果 - Eric Venner

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  1. 1
    Empowering personalized pharmacogenomics with generative AI solutions

    Empowering personalized pharmacogenomics with generative AI solutions 由 Mullai Murugan, Bo Yuan, Eric Venner, Christie M. Ballantyne, Katherine M. Robinson, James C. Coons, Liwen Wang, Philip E. Empey, Richard A. Gibbs

    出版 2024
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  2. 2
    Artificial Intelligence and Cardiovascular Genetics

    Artificial Intelligence and Cardiovascular Genetics 由 Chayakrit Krittanawong, Kipp W. Johnson, Edward Choi, Scott Kaplin, Eric Venner, Mullai Murugan, Zhen Wang, Benjamin S. Glicksberg, Christopher I. Amos, Michael C. Schatz, W.H. Wilson Tang

    出版 2022
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  3. 3
    Exome variant discrepancies due to reference-genome differences

    Exome variant discrepancies due to reference-genome differences 由 Li He, Moez Dawood, Michael M. Khayat, Jesse Farek, Shalini N. Jhangiani, Ziad Khan, Tadahiro Mitani, Zeynep Coban‐Akdemir, James R. Lupski, Eric Venner, Jennifer E. Posey, Aniko Sabo, Richard A. Gibbs

    出版 2021
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  4. 4
    The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities

    The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities 由 Eric Venner, Karynne Patterson, Divya Kalra, Marsha M. Wheeler, Yi‐Ju Chen, Sara E. Kalla, Bo Yuan, Jason H. Karnes, Kimberly Walker, Joshua D. Smith, Sean McGee, Aparna Radhakrishnan, Andrew Haddad, Philip E. Empey, Qiaoyan Wang, Lee Lichtenstein, Diana Toledo, Gail P. Jarvik, Anjene Musick, Richard A. Gibbs

    出版 2024
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  5. 5
    Novel Genetic Triggers and Genotype–Phenotype Correlations in Patients With Left Ventricular Noncompaction

    Novel Genetic Triggers and Genotype–Phenotype Correlations in Patients With Left Ventricular Noncompaction 由 Karol Miszalski‐Jamka, John L. Jefferies, Wojciech Mazur, Jan Głowacki, Jianhong Hu, Monika Lazar, Richard A. Gibbs, Jacek Liczko, Jan Kłyś, Eric Venner, Donna M. Muzny, Jarosław Rycaj, Jacek Białkowski, Ewa Kluczewska, Zbigniew Kalarus, Shalini N. Jhangiani, Hussein R. Al‐Khalidi, Tomasz Kukulski, James R. Lupski, William J. Craigen, Matthew N. Bainbridge

    出版 2017
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  6. 6
    Best practices for the interpretation and reporting of clinical whole genome sequencing

    Best practices for the interpretation and reporting of clinical whole genome sequencing 由 Christina Austin‐Tse, Vaidehi Jobanputra, Denise Perry, David Bick, Ryan J. Taft, Eric Venner, Richard A. Gibbs, Edwin J. Young, Sarah Barnett, John W. Belmont, Nicole J. Boczek, Shimul Chowdhury, Katarzyna A. Ellsworth, Saurav Guha, Shashikant Kulkarni, Cherisse A. Marcou, Linyan Meng, David R. Murdock, Atteeq U. Rehman, Elizabeth Spiteri, Amanda Thomas‐Wilson, Hutton M. Kearney, Heidi L. Rehm

    出版 2022
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  7. 7
    Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research Program

    Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research Program 由 Eric Venner, Donna M. Muzny, Joshua D. Smith, Kimberly Walker, Cynthia L. Neben, Christina M. Lockwood, Phillip E. Empey, Ginger Metcalf, Chris Kachulis, Shahzad I. Mian, Anjene Musick, Heidi L. Rehm, Steven M. Harrison, Stacey Gabriel, Richard A. Gibbs, Deborah A. Nickerson, Alicia Y. Zhou, Kimberly F. Doheny, Bradley A. Ozenberger, Scott Topper, Niall J. Lennon

    出版 2022
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  8. 8
    Variant Classification Concordance using the ACMG-AMP Variant Interpretation Guidelines across Nine Genomic Implementation Research Studies

    Variant Classification Concordance using the ACMG-AMP Variant Interpretation Guidelines across Nine Genomic Implementation Research Studies 由 Laura M. Amendola, Kathleen Muenzen, Leslie G. Biesecker, Kevin M. Bowling, Gregory M. Cooper, Michael O. Dorschner, Catherine C. Driscoll, Ann Katherine M. Foreman, Katie Golden‐Grant, John M. Greally, Lucia A. Hindorff, Dona Kanavy, Vaidehi Jobanputra, Jennifer J. Johnston, Eimear E. Kenny, Shannon McNulty, Priyanka Murali, Jeffrey Ou, Bradford C. Powell, Heidi L. Rehm, Bradley A. Rolf, Tamara S. Roman, Jessica Van Ziffle, Saurav Guha, Avinash Abhyankar, David R. Crosslin, Eric Venner, Bo Yuan, Hana Zouk, Gail P. Jarvik

    出版 2020
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  9. 9
    Association of Pathogenic Variants in Hereditary Cancer Genes With Multiple Diseases

    Association of Pathogenic Variants in Hereditary Cancer Genes With Multiple Diseases 由 Chenjie Zeng, Lisa A. Bastarache, Ran Tao, Eric Venner, Scott J. Hebbring, Justin Andujar, Harris T. Bland, David R. Crosslin, Siddharth Pratap, Ayorinde Cooley, Jennifer A. Pacheco, Kurt D. Christensen, Emma Perez, Carrie L. Blout Zawatsky, Leora Witkowski, Hana Zouk, Chunhua Weng, Kathleen A. Leppig, Patrick Sleiman, Hákon Hákonarson, Marc S. Williams, Yuan Luo, Gail P. Jarvik, Robert C. Green, Wendy K. Chung, Ali G. Gharavi, Niall J. Lennon, Heidi L. Rehm, Richard A. Gibbs, Josh F. Peterson, Dan M. Roden, Georgia L. Wiesner, Joshua C. Denny

    出版 2022
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  10. 10
    Improving reporting standards for polygenic scores in risk prediction studies

    Improving reporting standards for polygenic scores in risk prediction studies 由 Hannah Wand, Samuel A. Lambert, Cecelia P. Tamburro, Michael A. Iacocca, Jack W. O’Sullivan, Catherine H. Sillari, Iftikhar J. Kullo, Robb Rowley, Jacqueline S. Dron, Deanna Brockman, Eric Venner, Mark I. McCarthy, Antonis C. Antoniou, Douglas F. Easton, Robert A. Hegele, Amit V. Khera, Nilanjan Chatterjee, Charles Kooperberg, Karen L. Edwards, Katherine Vlessis, Kim Kinnear, John Danesh, Helen Parkinson, Erin M. Ramos, Megan C. Roberts, Kelly E. Ormond, Muin J. Khoury, A. Cecile J.W. Janssens, Katrina A.B. Goddard, Peter Kraft, Jacqueline MacArthur, Michael Inouye, Genevieve L. Wojcik

    出版 2021
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  11. 11
    Frequency of genomic secondary findings among 21,915 eMERGE network participants

    Frequency of genomic secondary findings among 21,915 eMERGE network participants 由 Allan Gordon, Hana Zouk, Eric Venner, Christine M. Eng, Birgit Funke, Laura M. Amendola, David Carrell, Rex L. Chisholm, Wendy K. Chung, Joshua C. Denny, Alexander Fedotov, Hákon Hákonarson, Iftikhar J. Kullo, Eric B. Larson, Magalie S. Leduc, Kathleen A. Leppig, Niall J. Lennon, Jodell E. Linder, Donna M. Muzny, Cynthia A. Prows, Laura J. Rasmussen‐Torvik, Hila Milo Rasouly, Dan M. Roden, Elisabeth A. Rosenthal, Maureen E. Smith, Ian B. Stanaway, Sara L. Van Driest, Kimberly Walker, Georgia L. Wiesner, Marc S. Williams, Leora Witkowski, David R. Crosslin, Richard A. Gibbs, Heidi L. Rehm, Gail P. Jarvik

    出版 2020
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  12. 12
    Cohort Profile: The Right Drug, Right Dose, Right Time: Using Genomic Data to Individualize Treatment Protocol (RIGHT Protocol)

    Cohort Profile: The Right Drug, Right Dose, Right Time: Using Genomic Data to Individualize Treatment Protocol (RIGHT Protocol) 由 Suzette J. Bielinski, Jennifer L. St. Sauver, Janet E. Olson, Nicholas B. Larson, John L. Black, Steven E. Scherer, Matthew Bernard, Eric Boerwinkle, Bijan J. Borah, Pedro J. Caraballo, Timothy B. Curry, HarshaVardhan Doddapaneni, Christine M. Formea, Robert R. Freimuth, Richard A. Gibbs, Jyothsna Giri, Matthew Hathcock, Jianhong Hu, Debra J. Jacobson, Leila A. Jones, Sara E. Kalla, Tyler Koep, Viktoriya Korchina, Christie Kovar, Charles Lee, Hongfang Liu, Eric T. Matey, Michaela E. McGree, Tammy M. McAllister, Ann M. Moyer, Donna M. Muzny, Wayne T. Nicholson, Lance J. Oyen, Xiang Qin, Ritika Raj, Véronique L. Roger, Carolyn R. Rohrer Vitek, Jason Ross, Richard R. Sharp, Paul Y. Takahashi, Eric Venner, Kimberly Walker, Liwei Wang, Qiaoyan Wang, Jessica Wright, Tsung-Jung Wu, Liewei Wang, Richard M. Weinshilboum

    出版 2019
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  13. 13
    A large-scale evaluation of computational protein function prediction

    A large-scale evaluation of computational protein function prediction 由 Predrag Radivojac, Wyatt T. Clark, Tal Oron, Alexandra M. Schnoes, Tobias Wittkop, Artem Sokolov, Kiley Graim, Christopher S. Funk, Karin Verspoor, Asa Ben‐Hur, Gaurav Pandey, Jeffrey M. Yunes, Ameet Talwalkar, Susanna Repo, Michael L Souza, Damiano Piovesan, Rita Casadio, Zheng Wang, Jianlin Cheng, Hai Fang, Julian Gough, Patrik Koskinen, Petri Törönen, Jussi Nokso-Koivisto, Liisa Holm, Domenico Cozzetto, Daniel Buchan, Kevin Bryson, David T. Jones, Bhakti Limaye, Harshal Inamdar, Avik Datta, Sunitha K Manjari, Rajendra Joshi, Meghana Chitale, Daisuke Kihara, Andreas Martin Lisewski, Serkan Erdin, Eric Venner, Olivier Lichtarge, Robert Rentzsch, Haixuan Yang, Alfonso E. Romero, Prajwal Bhat, Alberto Paccanaro, Tobias Hamp, Rebecca Kaßner, Stefan Seemayer, Esmeralda Vicedo, Christian Schaefer, Dominik Achten, Florian Auer, Ariane C. Boehm, Tatjana Braun, Maximilian Hecht, B. Mark Heron, Peter Hönigschmid, Thomas A. Hopf, Stefanie Kaufmann, Michael Kiening, Denis Krompaß, Cedric Landerer, Yannick Mahlich, Manfred Roos, Jari Björne, Tapio Salakoski, Andrew Wong, Hagit Shatkay, Fanny Gatzmann, I. Sommer, Mark N. Wass, Michael J.E. Sternberg, Nives Škunca, Fran Supek, Matko Bošnjak, Panče Panov, Sašo Džeroski, Tomislav Šmuc, Yiannis Kourmpetis, Aalt D. J. van Dijk, Cajo J. F. ter Braak, Yuanpeng Zhou, Qingtian Gong, Xinran Dong, Weidong Tian, Marco Falda, Paolo Fontana, Enrico Lavezzo, Barbara Di Camillo, Stefano Toppo, Liang Lan, Nemanja Djuric, Yuhong Guo, Slobodan Vučetić, Amos Bairoch, Michal Linial, Patricia C. Babbitt, Steven E. Brenner, Christine Orengo, Burkhard Rost

    出版 2013
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  14. 14
    Genomic data in the All of Us Research Program

    Genomic data in the All of Us Research Program 由 Alexander G. Bick, Ginger Metcalf, Kelsey Mayo, Lee Lichtenstein, Shimon Rura, Robert J. Carroll, Anjene Musick, Jodell E. Linder, I. King Jordan, Shashwat Deepali Nagar, Shivam Sharma, Robert Meller, Melissa Basford, Eric Boerwinkle, Mine Cicek, Kimberly F. Doheny, Evan E. Eichler, Stacey Gabriel, Richard A. Gibbs, David Glazer, Paul A. Harris, Gail P. Jarvik, Anthony Philippakis, Heidi L. Rehm, Dan M. Roden, Stephen N. Thibodeau, Scott Topper, Ashley L. Blegen, Samantha J. Wirkus, Victoria A. Wagner, Jeffrey G. Meyer, Mine Cicek, Donna M. Muzny, Eric Venner, Michelle Mawhinney, Sean Griffith, Elvin Hsu, Hua Ling, Marcia K. Adams, Kimberly Walker, Taobo Hu, HarshaVardhan Doddapaneni, Christie Kovar, Mullai Murugan, Shannon Dugan, Ziad Khan, Eric Boerwinkle, Niall J. Lennon, Christina Austin‐Tse, Eric Banks, Michael Gatzen, Namrata Gupta, Emma Henricks, Katie Larsson, Sheli McDonough, Steven M. Harrison, Christopher Kachulis, Matthew S. Lebo, Cynthia L. Neben, Marcie Steeves, Alicia Y. Zhou, Joshua D. Smith, Christian D. Frazar, Colleen Davis, Karynne Patterson, Marsha M. Wheeler, Sean McGee, Christina M. Lockwood, Brian H. Shirts, Colin C. Pritchard, Mitzi L. Murray, Valeria Vasta, Dru F. Leistritz, M Richardson, Jillian G. Buchan, Aparna Radhakrishnan, Niklas Krumm, Brenna Ehmen, Sophie Schwartz, M. Morgan T. Aster, Kristian Cibulskis, Andrea Haessly, Rebecca Asch, Aurora Cremer, Kylee Degatano, Akum Shergill, Laura D. Gauthier, Samuel K. Lee, Aaron Hatcher, George Grant, Genevieve R. Brandt, Miguel Covarrubias, Eric Banks, Ashley Able, Ashley E. Green, Robert J. Carroll, Jennifer Zhang, Henry Robert Condon, Y. Wang, Moira K. Dillon

    出版 2024
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  15. 15
    Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network

    Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network 由 Hana Zouk, Eric Venner, Niall J. Lennon, Donna M. Muzny, Debra Abrams, Samuel E. Adunyah, Ladia Albertson‐Junkans, Darren C. Ames, Paul S. Appelbaum, Samuel Aronson, Sharon Aufox, Lawrence Babb, Adithya Balasubramanian, Hana Bangash, Melissa Basford, Lisa Bastarache, Samantha Baxter, Meckenzie Behr, Barbara Benoit, Elizabeth Bhoj, Suzette J. Bielinski, Harris T. Bland, Carrie L. Blout Zawatsky, Kenneth M. Borthwick, Erwin P. Böttinger, Mark Bowser, Harrison Brand, Murray H. Brilliant, Wendy Brodeur, Pedro J. Caraballo, David Carrell, Andrew Carroll, Berta Almoguera, Lisa Castillo, Víctor M. Castro, Gauthami Chandanavelli, Theodore Chiang, Rex L. Chisholm, Kurt D. Christensen, Wendy K. Chung, Christopher G. Chute, Brittany City, Beth L. Cobb, John J. Connolly, Paul K. Crane, Katherine D. Crew, David R. Crosslin, Mariza de Andrade, Jessica De la Cruz, Shawn Denson, Joshua C. Denny, Tim DeSmet, Ozan Dikilitas, Christopher A. Friedrich, Stephanie M. Fullerton, Birgit Funke, Stacey Gabriel, Vivian S. Gainer, Ali G. Gharavi, Andrew M. Glazer, Joseph Glessner, Jessica Goehringer, Allan Gordon, Chet Graham, Robert C. Green, Justin H. Gundelach, Jyoti G. Dayal, Heather S. Hain, Hákon Hákonarson, Maegan Harden, John B. Harley, Margaret Harr, Andrea L. Hartzler, M. Geoffrey Hayes, Scott J. Hebbring, Nora B. Henrikson, Andrew D. Hershey, Christin Hoell, Ingrid A. Holm, Kayla M. Howell, George Hripcsak, Jianhong Hu, Gail P. Jarvik, Joy C. Jayaseelan, Yunyun Jiang, Yoonjung Yoonie Joo, Sheethal Jose, Navya Shilpa Josyula, Anne E. Justice, Sara E. Kalla, Divya Kalra, Elizabeth W. Karlson, Melissa Kelly, Brendan J. Keating, Eimear E. Kenny, Dustin Key, Krzysztof Kiryluk, Terrie Kitchner, Barbara J. Klanderman, Eric W. Klee

    出版 2019
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  16. 16
    Implementation of preemptive DNA sequence–based pharmacogenomics testing across a large academic medical center: The Mayo-Baylor RIGHT 10K Study

    Implementation of preemptive DNA sequence–based pharmacogenomics testing across a large academic medical center: The Mayo-Baylor RIGHT 10K Study 由 Liewei Wang, Steven E. Scherer, Suzette J. Bielinski, Donna M. Muzny, Leila A. Jones, John L. Black, Ann M. Moyer, Jyothsna Giri, Richard R. Sharp, Eric T. Matey, Jessica Wright, Lance J. Oyen, Wayne T. Nicholson, Mathieu Wiepert, Terri Sullard, Timothy B. Curry, Carolyn R. Rohrer Vitek, Tammy M. McAllister, Jennifer L. St. Sauver, Pedro J. Caraballo, Konstantinos N. Lazaridis, Eric Venner, Xiang Qin, Taobo Hu, Christie Kovar, Viktoriya Korchina, Kimberly Walker, HarshaVardhan Doddapaneni, Tsung-Jung Wu, Ritika Raj, Shawn Denson, Wen Liu, Gauthami Chandanavelli, Lan Zhang, Qiaoyan Wang, Divya Kalra, Mary Beth Karow, Kimberley Harris, Hugues Sicotte, Sandra E. Peterson, Amy E. Barthel, Brenda E. Moore, Jennifer M. Skierka, Michelle L. Kluge, Katrina E. Kotzer, Karen M. Kloke, Jessica M. Vander Pol, Heather Marker, Joseph Sutton, Adrijana Kekić, Ashley Ebenhoh, Dennis M. Bierle, Michael J. Schuh, C. Grilli, Sara M. Erickson, Audrey Umbreit, Leah Ward, Sheena Crosby, Eric Nelson, Sharon Levey, Michelle A. Elliott, Steve G. Peters, Naveen L. Pereira, Mark A. Frye, Fadi Shamoun, Matthew P. Goetz, Iftikhar J. Kullo, Robert A. Wermers, Jan A. Anderson, Christine M. Formea, Razan M. El Melik, John D. Zeuli, Joseph R. Herges, Carrie A. Krieger, Robert W. Hoel, Jodi L. Taraba, Scott R. St. Thomas, Imad Absah, Matthew Bernard, Stephanie Fink, Andrea A. Gossard, Pamela L. Grubbs, Therese M. Jacobson, Paul Y. Takahashi, Sharon C. Zehe, Susan Buckles, Michelle Bumgardner, Colette Gallagher, Kelliann C. Fee-Schroeder, Nichole R. Nicholas, Melody L. Powers, Ahmed K. Ragab, Darcy M. Richardson, Anthony Stai, Jaymi Wilson, Joel E. Pacyna, Janet E. Olson, Erica J. Sutton, Annika T. Beck, Caroline Horrow

    出版 2022
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